EP2804917B1 - Trockene siloxanbasierte löschbare beschichtungen mit geringem gehalt an flüchtigen organischen komponenten - Google Patents

Trockene siloxanbasierte löschbare beschichtungen mit geringem gehalt an flüchtigen organischen komponenten Download PDF

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Publication number
EP2804917B1
EP2804917B1 EP13738034.1A EP13738034A EP2804917B1 EP 2804917 B1 EP2804917 B1 EP 2804917B1 EP 13738034 A EP13738034 A EP 13738034A EP 2804917 B1 EP2804917 B1 EP 2804917B1
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EP
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Prior art keywords
less
coating
paint composition
cycles
cure
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EP13738034.1A
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English (en)
French (fr)
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EP2804917A1 (de
EP2804917A4 (de
Inventor
Frank C. Nachtman
Kristopher M. Felice
Adam W. EMERSON
Martin Douglas DONBROSKY, Jr.
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IdeaPaint Inc
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IdeaPaint Inc
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    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B43—WRITING OR DRAWING IMPLEMENTS; BUREAU ACCESSORIES
    • B43L—ARTICLES FOR WRITING OR DRAWING UPON; WRITING OR DRAWING AIDS; ACCESSORIES FOR WRITING OR DRAWING
    • B43L1/00—Repeatedly-usable boards or tablets for writing or drawing
    • B43L1/002—Repeatedly-usable boards or tablets for writing or drawing chemical details
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B43—WRITING OR DRAWING IMPLEMENTS; BUREAU ACCESSORIES
    • B43L—ARTICLES FOR WRITING OR DRAWING UPON; WRITING OR DRAWING AIDS; ACCESSORIES FOR WRITING OR DRAWING
    • B43L1/00—Repeatedly-usable boards or tablets for writing or drawing
    • B43L1/04—Blackboards
    • B43L1/10—Writing surfaces thereof
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
    • C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
    • C08G59/40—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
    • C08G59/50—Amines
    • C08G59/504—Amines containing an atom other than nitrogen belonging to the amine group, carbon and hydrogen
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D163/00—Coating compositions based on epoxy resins; Coating compositions based on derivatives of epoxy resins
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D183/00—Coating compositions based on macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon, with or without sulfur, nitrogen, oxygen, or carbon only; Coating compositions based on derivatives of such polymers
    • C09D183/04—Polysiloxanes
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
    • C08G77/42—Block-or graft-polymers containing polysiloxane sequences
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L63/00—Compositions of epoxy resins; Compositions of derivatives of epoxy resins
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
    • C08L83/04—Polysiloxanes
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
    • C08L83/04—Polysiloxanes
    • C08L83/06—Polysiloxanes containing silicon bound to oxygen-containing groups
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/31504—Composite [nonstructural laminate]
    • Y10T428/31511—Of epoxy ether

Definitions

  • EP 2 208 766 relates to water-based coatings having writable-erasable surfaces.
  • the coatings have many desirable attributes. For example, the coatings cure under ambient conditions, have low or no VOC emissions during and upon curing, and have reduced tendency to form ghost images, even after prolonged normal use.
  • the present invention encompasses the recognition of certain problems with coating materials that have write-erase character.
  • the invention provides particular insights with respect to siloxane compound-containing materials, popular in the coatings industry because of excellent resistance to radiation (e.g., ultraviolet light), to chemical breakdown, and to chalking, in addition to their environmental compatibility.
  • Siloxane compounds generally have low viscosities and can be used to prepare coatings with high solids content and relatively low volatile organic components (VOCs), and have been used to coat such items as storage tank exteriors, offshore platforms, bridges, exteriors of ships, hopper cars and exteriors of railway coaches.
  • the present invention relates to a particular set of siloxane compound-containing materials; those that cure to form a surface with write-erase characteristics.
  • the present invention identifies challenges in providing materials with sufficient hydrophobicity to achieve dry-erase character (e.g., resistance to penetration from marker solvents and/or pigments) that do not include unacceptably high (i.e., above 100 g/L, or even 140 g/L) levels of volatile organic components.
  • the present invention specifically provides siloxane compound-containing materials that cure to form dry-erase coatings and that contain less than 140 g/L, or less than 100 g/L VOCs.
  • provided siloxane compound-containing materials cure to form dry erase coatings characterized in that marks made on the coating surface marking material can be erased from the coating to be effectively invisible, resulting in little or no ghosting, even after prolonged normal use, for example.
  • provided siloxane compound-containing materials cure to form dry-erase coatings that maintain their character after about 10 cycles, after about 50 cycles, after about 100 cycles, after about 500 cycles, after about 1,000 cycles, after about 2,000 cycles, after about 3,000 cycles, after about 4,000 cycles, after about 5,000 cycles, after about 6,000 cycles, after about 7,000 cycles, after about 8,000 cycles, or after about 9,000 cycles of writing and erasing at the same position.
  • provided siloxane compound-containing materials show desired performance in specific write-erase tests.
  • provided siloxane compound-containing materials cure to a write-erase surface characterized by one or more of 1) average surface roughness (Ra) of less than about 7,500 nm; 2) a maximum surface roughness (Rm) of less than about 10,000 nm, 3) a 60 degree gloss of higher than 70; 4) a contact angle of less than about 150 degrees 5) a porosity of less than about 45 percent; 6) an elongation at break of between about 10 percent and about 100 percent; 7) a Sward hardness of greater than about 3; 8) a Taber abrasion value of less than about 150 mg/thousand cycles; and/or 9) a sag resistance of between about 4 mils and about 24 mils.
  • a "dry-erase”/"write-erase” material as described herein is characterized by a soak time as defined herein of at least about 4. In some embodiments, a "dry-erase”/"write-erase” material as described herein is characterized by one or more of the characteristics described herein.
  • “Curing” as used herein, refers to a process of setting (e.g., by evaporation (drying) and/or cross-linking) a material to form a coating on a substrate.
  • curing includes and/or is performed by exposure to ambient conditions, heat, radiation, and/or by cross-linking (e.g., oxidative cross-linking).
  • solvent-based refers to compositions including solvents, where the solvents in the composition are predominantly organic solvents. Such organic solvents may be used either in their anhydrous or wet form unless specified otherwise. In many embodiments, the term is particularly applied to liquid compositions.
  • Substantially solventless is used herein to refer to compositions in which solvents are present at a level below about 10%, and in some embodiments below about 5% by weight/volume of the composition. In many embodiments, the term is particularly applied to liquid compositions.
  • solventless is used herein to refer to compositions in which solvents are present at a level below about 1% by weight/volume of the liquid coating composition before application to a substrate. In many embodiments, the term is particularly applied to liquid compositions.
  • Ambient conditions refers to nominal, earth-bound conditions as they exist at sea level at a temperature of about 45-130°F.
  • ambient conditions include a temperature within the range of 20-25°C, and a pressure around 100 kPa.
  • Effectively invisible refers to a color difference Delta E (AE) of less than 20 as calculated according to the ASTM Test Method D2244 before and after a mark is erased by an eraser.
  • Substantially invisible refers to a color difference Delta E (AE) of less than 10 as calculated according to the ASTM Test Method D2244 before and after a mark is erased by an eraser.
  • Alkyl refers to a saturated or unsaturated hydrocarbon containing 1-20 carbon atoms including both acyclic and cyclic structures (such as methyl, ethyl, propyl, isopropyl, butyl, iso-butyl, sec-butyl, pentyl, hexyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, propenyl, butenyl, cyclohexenyl, and the like).
  • a linking divalent alkyl group is referred to as an "alkylene” (such as ethylene, propylene, and the like).
  • aryl refers to monocyclic or polycyclic (e.g., having 2, 3, or 4 fused rings) aromatic hydrocarbons such as, phenyl, naphthyl, anthracenyl, phenanthrenyl, indanyl, indenyl, and the like. In some embodiments, aryl groups have from 6 to 20 carbon atoms, from 6 to 15 carbon atoms, or from 6 to 10 carbon atoms.
  • heteroaryl refers to an aromatic heterocycle having at least one heteroatom ring atom such as sulfur, oxygen, or nitrogen.
  • Heteroaryl groups include monocyclic and polycyclic (e.g., having 2, 3, or 4 fused rings) systems. Examples of heteroaryl groups include without limitation, pyridyl, furyl, quinolyl, indolyl, oxazolyl, triazolyl, tetrazolyl, and the like.
  • the heteroaryl group has from 1 to 20 carbon atoms (e.g., from 3 to 20 carbon atoms).
  • the heteroaryl group has 1 to 4 heteroatoms (e.g., 1 to 3, or 1 to 2 heteroatoms).
  • aralkyl refers to alkyl substituted by aryl.
  • An example aralkyl group is benzyl.
  • alkoxy refers to an -0- alkyl group.
  • Example alkoxy groups include methoxy, ethoxy, propoxy (e.g., n-propoxy and isopropoxy), t-butoxy, and the like.
  • oxyalkylene refers to an -0- alkylene group.
  • alkoxylate refers to an alkyl-C(O)O.
  • Example alkoxylates include acetate, stearate, and the like.
  • halo includes fluoro, chloro, bromo, and iodo.
  • a "polyol” as used herein is a moiety that includes at least two hydroxyl (-OH) groups.
  • the hydroxyl groups can be terminal and/or non-terminal.
  • the hydroxyl groups can be primary hydroxyl groups.
  • polyurethane as used herein is a polymeric or oligomeric material that includes a urethane linkage in its backbone.
  • epoxy means an epoxy or polyepoxide polymer, including monomers or short chain polymers with an epoxide group at either end.
  • silane compound is used to refer to any substituted or unsubstituted silane.
  • a silane is a chemical compound containing both silicon and hydrogen, that is an analog of an alkane hydrocarbon. That is, a silanes consists of a chain of silicon atoms covalently bonded to each other and to hydrogen atoms.
  • the general formula of a silane is Si n H 2n+2 .
  • a "substituted silane” has a chemical structure that is related to that of a corresponding silane except that one or more of the hydrogen atoms has been substituted with a different chemical moiety.
  • a substituted silane for use in accordance with the present invention is a compound whose chemical structure is identical to that of a corresponding silane except that one or more hydrogens on the silane has/have been substituted with a moiety containing an amino group or a hydroxyl group, or both.
  • a substituted silane for use in accordance with the present invention contains one or more substituents (as compared with a reference silane) selected from the group consisting of amines, alcoholos, etc.; particular exemplary such groups include, for example, aminoethyl, methoxy, ethoxy, etc.
  • a substituted silane for use in accordance with the present invention is an aminosilane.
  • DYNASYLAN DAMO 2-amnoethyl-3-aminopropyl trimethoxysilane
  • siloxane compound encompasses siloxanes and polysiloxanes, and includes both branched and unbranched compounds, as well as side-chain-containing (e.g., organic-side-chain-containing) compounds.
  • a "siloxane” is a chemical compound composed of units of the form R 2 SiO, where R is a hydrogen atom or a hydrocarbon group. Siloxanes are generally recognized to belong to the wider class of organosilicon compounds.
  • Siloxanes for use in accordance with the present invention can have branched or unbranched backbones consisting of alternating silicon and oxygen atoms -Si-O-Si-O-, with side chains R attached to the silicon atoms. More complicated structures are also known, for example, eight silicon atoms at the corners of a cube connected by 12 oxygen atoms as the cube edges. Further, the term as used herein includes polymerized siloxanes, which may have organic side chains (R H), and are referred to in the art as silicones or as polysiloxanes.
  • substituted refers to a chemical compound having a structure identical to that of a reference compound except that one or more moieties of the reference compound has been "substituted” with a substituent moiety.
  • the structures of the substituted compound and reference compound are identical except that one or more hydrogen atoms in the reference compound has been substituted with a substituent moiety.
  • a substitutent moiety can be any chemical entity that can bond to the rest of the molecule consistent with rules of chemical bonding.
  • a substitutent moiety has fewer than 100, 95, 90, 85, 80, 75, 70, 65, 60, 55, 50, 45, 40, 35, 30, 25, 20, 15, 10 atoms.
  • a product or material described herein is considered to be a "dry-erase” or “write-erase”, which terms are used interchangeably, if it is characterized in that it can be written on using a marking materials as discussed below, and such writing can be removed substantially completely with minimal effort and without the use of an applied solvent.
  • a material is considered to be "write-erase” or “dry-erase” if a marking material can be erased from the material to be effectively invisible, resulting in little or no ghosting, even after prolonged normal use, for example, after about 10 cycles (e.g., after about 50 cycles, after about 100 cycles, after about 500 cycles, after about 1,000 cycles, after about 2,000 cycles, after about 3,000 cycles, after about 4,000 cycles, after about 5,000 cycles, after about 6,000 cycles, after about 7,000 cycles, after about 8,000 cycles, or after about 9,000 cycles) of writing and erasing at the same position and/or have desired performance in specific write-erase tests.
  • cycles e.g., after about 50 cycles, after about 100 cycles, after about 500 cycles, after about 1,000 cycles, after about 2,000 cycles, after about 3,000 cycles, after about 4,000 cycles, after about 5,000 cycles, after about 6,000 cycles, after about 7,000 cycles, after about 8,000 cycles, or after about 9,000 cycles
  • a "dry-erase”/"write-erase” material as described herein is characterized by one or more of 1) average surface roughness (Ra) of less than about 7,500 nm; 2) a maximum surface roughness (Rm) of less than about 10,000 nm; 3) a 60 degree gloss of higher than 70; 4) a contact angle of less than about 150 degrees; 5) a porosity of less than about 45 percent; 6) an elongation at break of between about 10 percent and about 200 percent; 7) a Sward hardness of greater than about 3; 8) a Taber abrasion value of less than about 150 mg/thousand cycles; and/or 9) a sag resistance of between about 4 mils and about 24 mils.
  • a "dry-erase”/"write-erase” material as described herein is characterized by a soak time as defined herein of at least about 4. In some embodiments, a "dry-erase”/"write-erase” material as described herein is characterized by one or more of the characteristics described herein.
  • coatings herein provide writable-erasable surfaces on a substrate.
  • provided coatings are produced from one or more materials in an essentially solventless, or substantially solventless system as defined herein.
  • provided coatings form by curing cure under ambient conditions.
  • provided coatings cure faster and/or more completely in the presence of light, heat, and/or other types of radiation.
  • the marking material can be erased to be effectively invisible (e.g., substantially invisible) with little or no ghosting, even after prolonged and repeated use.
  • the one or more materials that form the coatings emit minimal volatile organic compounds (VOCs) after curing on the substrate.
  • the cured coating includes less than about 100g/L or 140 g/L of volatile organic compounds ("VOC").
  • VOC volatile organic compounds
  • the resulting coatings have many desirable attributes, including one or more of the following: low porosity, low surface roughness, high elongation at break, high Taber abrasion resistance, and high Sward hardness.
  • the low porosity of provided coatings makes them substantially impervious to the marking materials, while the low surface roughness prevents the marking materials from becoming entrapped on the surface beyond effective reach of an eraser.
  • the marking material can be erased from the writable-erasable surface to be effectively invisible (e.g., substantially invisible).
  • a writable-erasable product includes a cured coating (such as a cross-linked coating) extending upon a substrate and having a writable-erasable surface.
  • a coating material is applied to the surface as a substantially solventless liquid composition, wherein the liquid carrier is a combination of liquid and solid starting materials, but does not include and/or does not require addition of, an organic solvent (such as an alcohol, aceton, ketone, or other organic solvent).
  • an organic solvent such as an alcohol, aceton, ketone, or other organic solvent.
  • such a coating material does not contain and/or does not require addition of more than about 10% by weight of water.
  • An applied coating composition can be cured while on a substrate under ambient conditions.
  • exemplary coatings and/or coating compositions can be formed from one or more parts (e.g., components) each independently including one or more ingredients.
  • one or both of the component compositions contains at least one siloxane compound.
  • a siloxane-compound or siloxane-compound-containing material e.g., a siloxane-compound-containing component
  • siloxane compounds herein, and/or compositions comprising them can be provided as liquids, solids, or any combination thereof (powders, solutions, suspensions, mixtures, etc.).
  • siloxane compounds appropriate for use in accordance with the present invention can, for example, be or comprise one or more cyclic siloxane compounds such as hexamethylcyclotrisiloxane, octamethylcyclotetrasiloxane, decamethylcyclopentasiloxane and dodecamethylcyclohexasiloxane, and/or one or more linear siloxane compounds such as hexamethyldisiloxane, octamethyltrisiloxane, decamethyltetrasiloxane and polydimethylsiloxane.
  • cyclic siloxane compounds such as hexamethylcyclotrisiloxane, octamethylcyclotetrasiloxane, decamethylcyclopentasiloxane and dodecamethylcyclohexasiloxane
  • linear siloxane compounds such as hexamethyldisiloxane, octamethyltrisi
  • coating compositions comprising one or more materials including one or more siloxane compounds.
  • Exemplary coating compositions are generated by combining component formulations that include at least one resin part (as component A) and at least one cure part (as component B), the cure part including one or more of siloxane compounds.
  • one or more materials, ingredients, and/or components utilized to produce write erase coating compositions in accordance with the present invention can be in a liquid carrier.
  • the liquid carrier can be a result of mixing one or more starting materials that are present in a liquid physical state, and/or by combining one or more starting materials in a solid state with one or more starting materials in a liquid state.
  • some or all of the liquids used in accordance with the practice of the present invention are solventless.
  • Liquid or non-liquid starting materials can be mixed into a liquid state starting material to form either part/component - whether the resin part, or the cure part, or both.
  • a resin part and a cure part After a resin part and a cure part are mixed together, they form a coating composition that can be applied to the surface of a substrate to generate a coating that cures to form a writable-erasable surface.
  • the cure part has the effect of hardening the composition, whether by cross-linking or other chemical and physical processes.
  • the coating After curing, the coating is hard and smooth and substantially non-porous so that it can be marked with a marking material including a colorant and a solvent, and thereafter, the marking material can be erased from the writable-erasable surface to be effectively invisible (e.g., substantially invisible).
  • white coatings are preferable for "white boards"
  • the coating can be produced in any desirable color, such as by the addition of colorants and/or pigments to the liquid state composition before curing.
  • a method of making a writable-erasable product includes applying the coating described herein to a substrate and curing the coating (e.g., under ambient conditions) to provide a cured coating defining a writable-erasable surface.
  • a coating can be formed from one or more materials, components, or parts, each independently or collectively including one or more substances including any or all of: a silane, an epoxy, a siloxane, and optionally other ingredients such as UV absorbers, preservatives, and biocidal agents, for example.
  • one or more, one or materials are in form of resin solid (e.g., epoxy resin).
  • at least one of one or more of the materials can be provided in a liquid state.
  • one or more materials are provided in a solvent carrier, preferably using water as a solvent carrier, and less preferably using an organic solvent.
  • a composition can further optionally include additives such as a catalyst, a surface additive, a surfactant, a wetting agent, a defoaming agent, a pigment, a biocide, and/or a colorant.
  • additives such as a catalyst, a surface additive, a surfactant, a wetting agent, a defoaming agent, a pigment, a biocide, and/or a colorant.
  • a writable-erasable product including a cured coating extending upon a substrate and having a writable-erasable surface.
  • a coating composition described herein can be applied to a surface, so that the coating forms on the surface.
  • At least one of one or more materials used in preparing such coating compositions can be in a liquid state, for example in a substantially solventless carrier. curing, the resulting writable-erasable surface can bemarked with a marking material including a colorant and a solvent, and the marking material can be erased from the writable-erasable surface to be effectively invisible (e.g., substantially invisible).
  • a catalyst is included, preferably in at least one of the resin part or cure part, or both.
  • a catalyst is included in a cure part.
  • a catalyst can be or comprise a tin catalyst as discussed below.
  • a catalyst can be or comprise dibutyltin dilaurate (DBTDL).
  • DBTDL dibutyltin dilaurate
  • it is provided as triethylamine.
  • a UV absorber is also provided, preferably in a cure part. Sometimes, the UV absorber is provided as a sebacate, such as 1,2,2,6,6-pentamethyl-4-piperidyl sebacate ( CAS 41556-26-7 ).
  • the solvent can include one or more hydrocarbons (such as saturated hydrocarbons and unsaturated hydrocarbons), alcohols (such as alkoxy alcohols, ketonic alcohols), ketones, esters (such as acetates), mineral spirits, bio-based solvents, or mixtures thereof.
  • solvents can include ethyl benzene, toluene, xylene, naphtha (petroleum), petroleum distillates, n-butyl acetate, methyl iso-amyl ketone, Stoddard solvent, t-butyl acetate, acetone, isopropyl alcohol, 2-butoxyethanol, toluene, methanol, propanol, 2-butanol, iso-amyl alcohol, methyl amyl alcohol, pentane, heptane, odorless mineral spirits, methyl ethyl ketone, diacetone alcohol, methyl amyl ketone, ethyl amyl ketone, diisobutyl ketone, methyl heptyl ketone, ethyl acetate, isopropyl acetate, propyl acetate, isobutyl acetate, n-butyl acetate, glycol ether
  • a substrate can be selected from the group consisting of cellulosic material, glass, wall (such as plaster or painted wall), fiber board (e.g., a whiteboard in which the cured coating can be extending upon a fiber board), particle board (e.g., a chalkboard or blackboard), gypsum board, wood, plastics (such as high density polyethylene (HDPE), low density polyethylene (LDPE), or a acrylonitrile, butadiene, styrene (ABS)-based material), densified ceramics, stone (such as granite), and metal (such as aluminum or stainless steel).
  • the substrate can be selected from a flexible film or a rigid structure.
  • a marking material includes a solvent including water, alcohols (such as alkoxy alcohols, ketonic alcohols), ketones, esters (such as acetates), mineral spirits, bio-based solvents, or their mixtures.
  • the marking material can be erased from the writable-erasable surface to be effectively invisible by wiping the marks with an eraser including a fibrous material (such as a paper towel, rag, or felt material).
  • the eraser is dry or includes water, alcohol (e.g., ethanol, n-propanol, isopropanol, n-butanol, isobutanol, benzyl alcohol), alkoxy alcohol (e.g., 2-(n-propoxy)ethanol, 2-(nbutoxy)ethanol, 3-(n-propoxy)ethanol), ketone (e.g., acetone, methyl ethyl ketone, methyl nbutyl ketone), ketonic alcohol (e.g., diacetone alcohol), ester (e.g., methyl succinate, methyl benzoate, ethyl propanoate), acetate (e.g., methyl acetate, ethyl acetate, n-butyl acetate, t-butyl acetate), mineral spirit, or mixtures thereof.
  • alcohol e.g., ethanol, n-propanol, isopropanol, n-butano
  • a writable-erasable product can take the form of a whiteboard, in which the cured coating extends upon a fiberboard, can form a part of a wall e.g., of a structure, or can form a plurality of sheets, each sheet including a substrate (e.g., in the form of a paper) having the cured coating extending thereupon.
  • the one or more materials including the resin part prior to combining, can be in a first container, and the one or more materials including one or more cure parts can be in a second container.
  • a catalyst can be combined with the cure part prior to mixing with the resin part.
  • Embodiments and/or aspects may include one or more of the following advantages.
  • Coating surfaces are writable and erasable.
  • the coatings can provide writing surfaces that exhibit little or no image ghosting, even after prolonged normal use.
  • Coatings can be simple to prepare and can be applied to many different substrates, including both porous (e.g., paper) and non-porous substrates (e.g., densified ceramics).
  • Coatings can be applied to various substrates including, but not limited to, chalkboards (e.g., blackboards), whiteboards, drywalls, gypsum boards, plaster, and painted walls.
  • a solvent-based coatings can be applied on the substrate on-site rather than being manufactured in a factory.
  • Coatings can exhibit good adhesive strength to many substrates.
  • Coating components (prior to mixing) can have an extended shelf-life, e.g., up to about three years or even up to six years. Coatings can be readily resurfaced. Coatings can cure rapidly, e.g., in less than about 12 to 60 hours, and more preferably between about 24 to about 48 hours, under ambient conditions. Coatings can resist yellowing, as determined by ASTM method G-154, for an extended period of time (e.g., up to 2000 hours or even up to 5000 hours). Coatings do not require UV light or high-energy radiation, such as a beam of electrons, for curing.
  • Coatings can have a reduced tendency to run even when applied upon a vertical substrate. Surface gloss of the coatings can be readily adjusted. The writing surface of the coating can be projectable. Coatings can be hard. Coatings can be substantially impervious to organic solvents and/or inks. Coatings can have a low porosity. Surfaces of coatings can have a low roughness. Coatings can be impact resistant. Coatings can be made scratch and abrasion resistant. Coatings can be relatively low cost. The coatings can have a high chemical resistance.
  • a writable-erasable product 10 includes a substrate 12 and a coating 14 (e.g., a cured coating) extending upon the substrate 12.
  • the cured coating 14 has a writable-erasable surface 16.
  • the marking material can be erased from the writable-erasable surface to be effectively (e.g., substantially) invisible, resulting in little or no ghosting, even after prolonged normal use, for example, after about 10 cycles (e.g., after about 50 cycles, after about 100 cycles, after about 500 cycles, after about 1,000 cycles, after about 2,000 cycles, after about 3,000 cycles, after about 4,000 cycles, after about 5,000 cycles, after about 6,000 cycles, after about 7,000 cycles, after about 8,000 cycles, or after about 9,000 cycles) of writing and erasing at the same position.
  • 10 cycles e.g., after about 50 cycles, after about 100 cycles, after about 500 cycles, after about 1,000 cycles, after about 2,000 cycles, after about 3,000 cycles, after about 4,000 cycles, after about 5,000 cycles, after about 6,000 cycles, after about 7,000 cycles, after about 8,000 cycles, or after about 9,000 cycles
  • the visibility, or the lack thereof, of the erasing can be determined by measuring the color change (Delta E, ⁇ E) on the writable-erasable surface using a spectrophotometer (such as the SP-62 portable spectrophotometer available from X-Rite), after marking on the surface and erasing the marking.
  • the color change is a composite of three variables, lightness (L*), red/green value (a*), and yellow/blue value (b*).
  • the erasability characteristics of the writable erasable surface 16 can be defined in terms of the ⁇ E value.
  • the ⁇ E for the writable-erasable surface 16 after 5,000 cycles (or even after 10,000 cycles) can be less than about 50, e.g., less than about 40, less than about 30, less than about 20, less than about 10, less than about 9, less than about 8, less than about 7, less than about 6, less than about 5, less than about 4, less than about 3, less than about 2, or less than about 1.
  • the ⁇ E for the writable-erasable surface 16 after 5,000 cycles (or even after 10,000 cycles) can be in a range of about 0.1 to about 10.0, e.g., about 0.1 to about 0.5, about 0.5 to about 1.0, about 1.0 to about 1.5, about 1.5 to about 2.0, from about 2.0 to about 2.5, about 2.5 to about 3.0, about 3.0 to about 3.5, about 3.5 to about 4.0, about 4.0 to about 4.5, about 4.5 to about 5.0, about 5.0 to about 5.5, about 5.5 to about 6.0, about 6.0 to about 6.5, about 6.5 to about 7.0, about 7.0 to about 7.5, about 7.5 to about 8.0, about 8.0 to about 8.5, about 8.5 to about 9.0, about 9.0 to about 9.5, or about 9.5 to about 10.0.
  • the erasability characteristic maybe evaluated based on the differences in L* ( ⁇ L*), without attribution to color differences.
  • such an evaluation can be combined with an assessment of the progressive abrasion of the coating on an abrader, such as the Taber abrader 4360.
  • abrasion of a coating can be performed similar to the ASTM Method D4060.
  • the erasability characteristic as a function of the abrasion can be determined by abrading the writable-erasable surface 16 for a certain number of cycles and then measuring the change in lightness ( ⁇ L*) value after marking on the surface followed by erasing the marking.
  • a substrate with a cured coating can be loaded on an abrader and abrasive wheels can be rotated on the writable-erasable surface 16 for a certain number of cycles (e.g., about 50 cycles, about 100 cycles, about 150 cycles, about 200 cycles, about 500 cycles, or about 1,000 cycles).
  • a spectrophotometer such as the SP-62 portable spectrophotometer available from X-Rite
  • the writable-erasable surface 16 can be marked with a marking material (such as an Expo® 1 or Expo® 2, blue or black marker) and erased (such as with an Expo® felt dry eraser).
  • a spectrophotometer (such as the SP-62 portable spectrophotometer available from X-Rite) can be used to measure the L* value of the erased area (L* b ).
  • the ⁇ L* can be determined from the difference of L* a and L* b values.
  • the ⁇ L* value for the writable-erasable surface 16 after 1,000 cycles can be at least about 20, e.g., at least about 30, at least about 40, at least about 50, at least about 60, at least about 65, at least about 70, at least about 75, at least about 80, at least about 85, at least about 90, or at least about 99.
  • the ⁇ L* value for the writable-erasable surface 16 after 1,000 cycles can be at least about 65, e.g., at least about 67, at least about 69, at least about 71, at least about 73, at least about 75, at least about 77, at least about 79, at least about 81, at least about 83, at least about 85, at least about 87, at least about 89, or at least about 91.
  • the ⁇ L* value for the writable-erasable surface 16 after 1,000 cycles can be from about 65 to about 70, from about 70 to about 75, from about 75 to about 80, from about 80 to about 85, from about 85 to about 90, from about 90 to about 95, or from about 95 to about 99.
  • the marking material can be erased from the writable-erasable surface to be effectively (e.g., substantially) invisible.
  • a marking material can include a colorant (e.g., a pigment) and a solvent such as water, alcohol (such as alkoxy alcohol, ketonic alcohol), ketone, ester (such as acetate), mineral spirit, bio-based solvents (e.g., vegetable oil, corn oil, sunflower oil). Mixtures of any of the noted solvents can also be used. For example, mixtures of two, three, four or more of the noted solvents may be used. Bio-based solvents are alternatives to conventional organic solvents and can be obtained from agricultural products. Such solvents can provide lower volatile organic compounds in coatings and decreased environmental impact.
  • a marking material can be selected from any of the industry standard dry-erase markers.
  • the marking material can be erased from the writable-erasable surface 16 to be effectively (e.g., substantially) invisible by wiping the marks with an eraser that includes a fibrous material.
  • the eraser can be in the form of a disposable wipe, a cloth, or a supported (e.g., wood, plastic) felt.
  • the eraser can also include a solvent such as water, alcohols (e.g., alkoxy alcohols, ketonic alcohols), ketones, esters, (e.g., acetates), or mineral spirits. Mixtures of any two or more of these solvents can also be used.
  • Examples of alcohols that can be used in the marking material or the eraser include ethanol, n-propanol, iso-propanol, n-butanol, iso-butanol, benzyl alcohol, 2-(n-propoxy)ethanol, 2-(n-butoxy)ethanol and 3-(n-propoxy)ethanol.
  • Examples of ketones that can be used in the marking material or the eraser include acetone, methyl ethyl ketone and methyl nbutyl ketone.
  • Examples of esters that can be used in the marking material or the eraser include methyl acetate, ethyl acetate, n-butyl acetate, and t-butyl acetate.
  • compositions that form the coating 14 can be applied to many different types of substrates, including porous (e.g., paper) and non-porous substrates (e.g., densified ceramics).
  • the substrate 12 can be a flexible film or a rigid movable or immovable structure.
  • the substrate examples include, but not limited to, a polymeric material (such as a polyester or a polyamide), a cellulosic material (such as paper), glass, wood, plastics (such as HDPE, LDPE, or an ABS-based material), a wall (such as a plaster or painted wall), a fiber board (such as a whiteboard in which the cured coating extends upon a fiber board), a particle board, (such as a chalkboard or blackboard), a gypsum board, densified ceramics, stone (such as granite), and a metal (such as aluminum or stainless steel).
  • the substrate could be a newly built structure or even an old and worn out chalkboard, blackboard, or whiteboard.
  • the surface of the substrate can be cleaned by sanding the surface and priming the surface prior to application of the coating.
  • the surface can also be cleaned with a cleaning agent (e.g., acetone or a mild acid) in order to provide better adhesion of the coating to the surface.
  • a cleaning agent e.g., acetone or a mild acid
  • compositions that that form the coating 14, prior to the application on substrates can have a pot life which is the period during which the materials must be applied on the substrate.
  • the materials can have a pot life in a range of about 10 minutes to about 16 hours, for example, about 30 minutes to about 12 hours, about 60 minutes to about 8 hours, about 2 hours to about 4 hours, or about 1 hour to about 4 hours, or about 1 hour to about 2 hours.
  • the materials can have a pot life of greater than about 6 months, for example, about 12 months, about 18 months, about 24 months, about 30 months, or about 36 months.
  • the pot life of the composition after mixing the resin part and any cure part(s) is preferably in a range of about 4 to about 6 hours.
  • the curing can be facilitated by ultra-violet (UV) light, thermal means, initiators, electron-beams, and combinations thereof.
  • the coating 14 on the substrate 10 can cure under ambient conditions in from about 4 hours to about a week, e.g., from about 4 hours to about 24 hours, from about 8 hours to about 20 hours, from about 12 hours to about 16 hours, from about 1 day to about 7 days, from about 2 days to about 6 days, or from about 3 days to about 5 days.
  • the cured coating 14 can be generally stable and also emit little or no VOCs after curing. Curing under ambient conditions can reduce environmental impact and can make the materials safer to use.
  • the porosity of a coating can determine the amount of marking material that can be trapped in the coating. While not intending to be bound by any theory, it is believed that lower porosity of coatings can lead to better writable-erasable surfaces.
  • the coating 14 can have a porosity in a range of about 1 percent and about 40 percent, e.g., about 2 percent and about 35 percent, about 2.5 percent and about 30 percent, or about 3 percent and about 20 percent.
  • the coating 14 can have a porosity of less than about 40 percent, e.g., less than about 35 percent, less than about 30 percent, less than about 25 percent, less than about 20 percent, less than about 15 percent, less than about 10 percent, less than about 5 percent, or even less than about 2.5 percent.
  • a coating e.g., a cured coating
  • a porosity in a range of about 2 percent and about 45 percent, e.g., about 2.5 percent and about 35 percent, or about 3 percent and about 35 percent.
  • the coating can have a porosity of about 3 percent, about 33 percent, or about 34 percent.
  • Materials/parts/compositions/formulations used in preparing write-erase coatings in accordance with the present invention can be prepared by any of a variety of approaches, including often by standard techniques known to one skilled in the art.
  • predetermined amounts of one or more ingredient materials to be used can be mixed at required speeds in high shear dispersers until the materials are homogeneously dispersed.
  • the degree of dispersion of the materials and pigments can be determined with a Hegman gauge.
  • One or more additional ingredients (including all remaining ingredients, if desired, can be introduced, for example at a letdown stage to obtain a final formulation appropriate for packaging.
  • the two parts can be mixed thoroughly and can be allowed to stand for a period of time before being applied on a substrate.
  • a coating formulation can be applied on a substrate 12 in a single coat or multiple coats using a roller, a spray (such as an aerosol spray), a brush, or using other types of applicators. In some embodiments, it can be painted using a foam roller in a single coat.
  • the coating (e.g., before or after curing) 14 can have a thickness, T ( FIG. 1A ), in a range of e.g., about 0.001 inch and about 0.125 inch, e.g., about 0.002 inch and about 0.1 inch, about 0.004 inch and about 0.08 inch, about 0.006 inch and about 0.06 inch, about 0.008 inch and about 0.04 inch, or about 0.01 inch and about 0.02 inch).
  • the coating (e.g., before or after curing) 14 can have a thickness of greater than about 0.005 inch, e.g., greater than about 0.0075 inch or greater than about 0.010 inch. While not intending to be bound by any theory, it is believed that providing a uniform, adequate coating thickness, T, reduces the likelihood of thin or uncoated substrate portions where marking materials might penetrate.
  • a coating (e.g., a cured coating) 14 can have a Taber abrasion value of less than about 150 mg/thousand cycles, e.g., less than about 100 mg/thousand cycles, less than about 75 mg/thousand cycles, less than about 50 mg/thousand cycles, less than about 35 mg/thousand cycles, less than about 25 mg/thousand cycles, less than about 15 mg/thousand cycles, less than about 10 mg/thousand cycles, less than about 5 mg/thousand cycles, less than about 2.5 mg/thousand cycles, less than about 1 mg/thousand cycles, or even less than about 0.5 mg/thousand cycles. Maintaining a low Taber abrasion value can provide long-lasting durability to the coating, reducing the incidence of thin spots which could allow penetration of marking material through the coating and into the substrate.
  • a coating (e.g., a cured coating) 14 can have a Sward hardness of greater than about 10, e.g., greater than about 15, greater than about 25, greater than about 50, greater than about 75, greater than about 100, greater than about 120, greater than about 150, or even greater than about 200.
  • Sward hardness of greater than about 10, e.g., greater than about 15, greater than about 25, greater than about 50, greater than about 75, greater than about 100, greater than about 120, greater than about 150, or even greater than about 200.
  • a coating (e.g., a cured coating) 14 can have a Sward hardness in a range of about 10 and about 75, e.g., about 15 and about 70 or about 15 and about 55. In some specific embodiments, the coating can have a Sward hardness of about 15, about 22 or about 25.
  • elongation at break for a coating can be in a range of about 5 percent and about 400 percent, e.g., about 25 percent and about 200 percent, or about 50 percent and about 150 percent. In other embodiments, the elongation at break can be greater than about 10 percent, e.g., greater than about 25 percent, greater than about 50 percent, or even greater than about 100 percent. While not intending to be bound by theory, it is believed that maintaining high elongation at break provides long-lasting durability to the coating and it allows the coating to be stressed without forming cracks. Cracks can trap marking materials making erasure from surfaces difficult and, hence, decreasing the longevity of the writable-erasable products.
  • sag resistance for a coating can be at least about 3 mils, e.g., about 4 mils, about 5 mils, about 6 mils, about 7 mils, about 8 mils, about 9 mils, about 10 mils, about 12 mils, about 14 mils, about 16 mils, about 18 mils, about 20 mils, about 22 mils, or about 24 mils.
  • the coating 14 can have a sag resistance in a range of about 4 mils to about 24 mils, e.g., about 5 mils to about 20 mils, about 6 mils to about 18 mils, about 7 mils to about 16 mils, about 8 mils to about 14 mils, about 9 mils to about 12 mils, or about 10 mils to about 12 mils.
  • a writable-erasable surface 16 can have an average surface roughness (Ra) in a range of about 0.5 nm and about 7,500 nm, e.g., about 1 nm and about 6,000 nm, about 2 nm and about 5,000 nm, about 5 nm and about 2,500 nm, about 10 nm and about 1,500 nm, about 20 nm and about 1,000 nm or about 25 nm and about 750 nm.
  • Ra surface roughness
  • the writable-erasable surface 16 can have an average surface roughness (R a ) of less than about 7,500 nm, e.g., less than about 5,000 nm, less than about 3,000 nm, less than about 2,000 nm, less than about 1,000 nm, less than about 500 nm, less than about 250 nm, less than about 200 nm, less than about 100 nm, or even less than about 50 nm.
  • R a average surface roughness
  • the writable-erasable surface 16 can have an average surface roughness (Ra) in a range of about 75 nm and about 1,000 nm, e.g., about 100 nm and about 500 nm or about 150 nm and about 400 nm. In certain embodiments, the writable-erasable surface 16 can have an average surface roughness (Ra) of about 150 nm, about 300 nm, or about 1,000 nm.
  • a writable-erasable surface 16 can have a maximum surface roughness (Rm) of less than about 10,000 nm, e.g., less than about 8,000 nm, less than about 6,500 nm, less than about 5,000 nm, less than about 3,500 nm, less than about 2,000 nm, less than about 1,000 nm, or less even than about 500 nm.
  • Rm maximum surface roughness
  • a writable-erasable surface 16 can have a flat finish (gloss below 15, measured at 85 degrees), an eggshell finish (gloss between about 5 and about 20, measured at 60 degrees), a satin finish (gloss between about 15 and about 35, measured at 60 degrees), a semi-gloss finish (gloss between about 30 and about 65, measured at 60 degrees), or gloss finish (gloss greater than about 65, measured at 60 degrees).
  • a writable-erasable surface 16 can have a 60 degree gloss in a range of about 45 and about 90, e.g., about 50 and about 85. In other embodiments, the writable-erasable surface 16 can have a 20 degree gloss in a range of about 10 and about 50, e.g., about 20 and about 45. In still other embodiments, the writableerasable surface 16 can have a 85 degree gloss in a range of about 45 and about 90, e.g., about 75 and about 90.
  • the writable-erasable surface 16 can have a 20 degree gloss of about 12, about 23, or about 46; or a 60 degree gloss of about 52, about 66, or about 85; or a 85 degree gloss of about 64, about 78, or about 88.
  • materials can be chosen so that a cured coating 14 has a surface that is relatively hydrophilic and not very hydrophobic.
  • hydrophobicity of the writable-erasable surface 16 is related to its wettability by a liquid, e.g., a water-based marking material. It is often desirable to quantify the hydrophobicity of the writable-erasable surface 16 by a contact angle.
  • 0 is 2x arctan(A/r), where A is the height of the droplet image, and r is half width at the base.
  • the writable-erasable surface 16 can be desirable for the writable-erasable surface 16 to have contact angle, 0, measured using deionized water of less than about 150 degrees e.g., less than about 125 degrees, less than about 100 degrees, less than about 75 degrees, or even less than about 50 degrees. In other embodiments, it can be desirable for the writable-erasable surface 16 to have contact angle 0 above about 35 degrees, e.g., above about 40 degrees, or above about 45 degrees.
  • contact angle 0, measured using deionized water, can be in a range of about 30 degrees and about 90 degrees, e.g., about 45 degrees and about 80 degrees, or about 39 degrees and about 77 degrees. In some specific embodiments, the contact angle can be about 40 degrees, for example, about 50 degrees, about 60 degrees, about 73 degrees, or about 77 degrees.
  • a writable-erasable surface 16 can have a surface tension in a range of about 30 dynes/cm and about 60 dynes/cm, e.g., about 40 dynes/cm and about 60 dynes/cm. In some embodiments, the writable-erasable surface 16 can have a surface tension of about 22 dynes/cm, about 25 dynes/cm, about 30 dynes/cm, about 42 dynes/cm, about 44 dynes/cm, or about 56 dynes/cm.
  • the writable-erasable surface 16 can have a surface tension more than about 22 dynes/cm, about 25 dynes/cm, about 30 dynes/cm, about 42 dynes/cm, about 44 dynes/cm, or about 56 dynes/cm.
  • a coating e.g., a cured coating
  • a coating 14 can be formed by applying (e.g., rolling, painting, or spraying) a solution of the material in a solvent-based carrier that can have a sufficient viscosity such that the applied coating 14 does not run soon after it is applied or during its curing. At the same time, the solution viscosity should be sufficient to permit easy application.
  • the applied solution can have a viscosity at 25°C in a range of about 75 mPas and about 20,000 mPas, e.g., about 200 mPas and about 15,000 mPas, about 1,000 mPas and about 10,000 mPas, or about 750 mPas and about 5,000 mPas.
  • a coating e.g., a cured coating
  • a coating 14 can be made by casting a material on a fluoropolymer substrate and then curing the material so that it can have a dry thickness of about 0.002 inch. The cured sample can then be removed from the fluoropolymer substrate to provide the test specimen. Testing can be performed at 25°C.
  • Elongation at break can be measured using ASTM method D-882; porosity can be measured using mercury porosimetry (suitable instruments available from Micromeritics, Norcross, Ga., e.g., Micromeritics Autopore IV 9500); surface roughness can be measured using atomic force microscopy (AFM) in tapping mode using ASME B46.1 (suitable instruments, e.g., WYKO NT8000, are available from Park Scientific); Taber abrasion resistance can be measured according to ASTM method D-4060 (wheel CS-17, 1 kg load) and Sward hardness can be measured according to ASTM method D-2134 (Sward Hardness Rocker Model C). VOC level(s) can be determined using the EPA Method 24.
  • Gloss can be measured using ASTM method D-523-89 (BYK Tri-Gloss Meter Cat. No. 4525). Contact angle can be measured with deionized water using the dynamic contact angle method (Angstroms Model FTA 200) using ASTM method D-5946-04. Sag resistance can be measured using ASTM method D4400 which can be performed by obtaining a draw-down and measuring visually by comparison with standard ASTM pictures. Surface tension can be measured using AccuDyne Marking Pens. Stormer Viscosity can be measured on a Brookfield Viscometer by ASTM method D-562 and reported in Kreb units (Ku).
  • the cured coating 14 having the writable-erasable surface 16 can be formed under ambient conditions from an uncured coating formulation.
  • the coating formulations in general, can include the materials described below.
  • formulations can be or include a one-component system and/or a multi-component system (e.g., a two-component system).
  • a coating composition and/or its parts will not cure if denied light and sealed in a substantially air-free container.
  • a one-component system for example, consists of a coating formulation material packaged to be ready for use.
  • a two-component system for example, consists of two coating materials that are mixed, upon demand and when desired, to obtain the final liquid coating formulation prior to application on the substrate.
  • a silane compound-based epoxy coating formulation can be obtained by mixing an epoxy resin with at least one siloxane compound (silicone, for example), and thereafter adding at least a cure part.
  • the silane compound-based epoxy resins can include polyether chains that contain one or more epoxide units in their structure. Polyethers have the repeating oxyalkylene units: alkylene substituted by oxygen groups, e.g., ethyleneoxy (-[CH 2 -CH 2 O]-). In some embodiments, the polyether chains can have additional functional groups such as hydroxyl (-OH). Curing of epoxy resins can lead to less amount of volatile products.
  • curing agents e.g., catalyst
  • curing agents in a cure part can be either nucleophilic or electrophilic.
  • nucleophilic agents include alcohols, phenols, amines, amino silanes, thiols, carboxylic acids, and acid anhydrides.
  • electrophilic agents include aryl iodonium salts, aryl sulfonium salts, and latent acid catalysts (e.g., dibutyltin diacetatonate CAS 22673-19-4 , aka 4-pentanedionato-o,o')-dibutyl bis (oc-6-11)- ti; dibutyl bis(2,4-pentanedionato-,o')-,(oc-6-11)-tin; di-n-butyltin bis(acetylacetonate), tech., 95%; di-n-butyltin bis(acetylacetonate); di-n-butyltin bis(2,4-pentanedionate); di-n-butyl bis(2,4-pentanedionate)tin; dibutyltin bis(acetylacetonate); dibutyltin bis(2,4-pentanedionate); dibut
  • curing agents can contain one or more nucleophilic groups.
  • Epoxy resins can contain an aliphatic (such as cyclic or acyclic) or an aromatic backbone or a combination of both. In some optional embodiments, the epoxy resins can contain other non-interfering chemical linkages (such as alkyl chains).
  • the coating 14 described in FIG. 1 can be formed from a resin part that includes an epoxy material and a silicon.
  • a silicon can be or comprise polysiloxane.
  • a silicon can be or comprise an organooxysilane.
  • Epoxy-polysiloxane polymers can be obtained by taking an epoxide resin having more than one 1,2-epoxy groups per molecule with an epoxide equivalent weight in the range of from 100 to about 2,000 that undergoes chain extension by reaction with the amine groups in a polysiloxane. Such polymers and processes are discussed below as described in U.S. Patent No. 5,618,860 and 5,275,645 .
  • Exemplary epoxide resins are non-aromatic hydrogenated cyclohexane dimethanol and diglycidyl ethers of hydrogenated Bisphenol A-type epoxide resin, such as Epon DPL-862, Eponex 1510, Heloxy 107 and Eponex 1513 (hydrogenated bisphenol A-epichlorohydrin epoxy resin) from Shell Chemical in Houston, Tex.; Santolink LSE-120 from Monsanto located in Springfield, Mass.; Epodil 757 (cyclohexane dimethanol diglycidylether) from Pacific Anchor located in Allentown, Pa.; Araldite XUGY358 and PY327 from Ciba Geigy located in Hawthorne, N.
  • a coating composition comprises in the range of from about 15 to about 45 percent by weight epoxide resin.
  • exemplary polysiloxanes include, but are not limited to, those having the following formula: R 2 -O-[Si(R 1 ) 2 -O] n -R 2 where each R 1 is selected from the group consisting of the hydroxy group and alkyl, aryl, and alkoxy groups having up to six carbon atoms. Each R 2 is selected from the group consisting of hydrogen and alkyl and aryl groups having up to six carbon atoms. In some embodiments, R 1 and R 2 comprise groups having less than six carbon atoms to facilitate rapid hydrolysis of the polysiloxane, which reaction is driven by the volatility of the alcohol analog product of the hydrolysis.
  • R 1 and R 2 groups having greater than six carbon atoms tend to impair the hydrolysis of the polysiloxane due to the relatively low volatility of each alcohol analog.
  • Methoxy, ethoxy and silanol functional polysiloxanes having n selected molecular weights are about 400 to about 2000 which are preferred for formulating coating and flooring materials of the present invention.
  • Methoxy, ethoxy and silanol functional polysiloxanes having molecular weights of less than 400 would produce a coating and flooring composition that would be brittle and offer poor impact resistance.
  • Methoxy, ethoxy and silanol functional polysiloxanes having molecular weights of greater than 2000 produce a coating and flooring composition having both a viscosity outside the desired range from about 3,000 to 15,000 centipoise (cP) at 20° C., and are too viscous for application without adding solvent in excess of current volatile organic content (VOC) requirements.
  • cP centipoise
  • exemplary methoxy functional polysiloxanes include DC-3074 and DC-3037 from Dow Corning; GE SR191 and SY-550 from Wacker located in Adrian, Mich.
  • Silanol functional polysiloxanes include, but are not limited to, Dow Coming's DC840, Z6018, Q1-2530 and 6-2230 intermediates.
  • a coating composition comprises in the range of from 15 to 45 percent by weight polysiloxane.
  • a flooring composition comprises in the range of from one to ten percent by weight polysiloxane. If the coating and flooring composition comprises an amount of polysiloxane outside each range, the coating and flooring composition produced will display inferior weatherability and chemical resistance.
  • a coating composition comprises approximately 30 percent by weight polysiloxane.
  • a flooring composition comprises approximately 3 percent by weight polysiloxane.
  • organooxysilanes have the general formula R 3 -Si-(OR 4 ) 3 where R 3 is selected from the group consisting of alkyl and cycloalkyl groups containing up to six carbon atoms and aryl groups containing up to ten carbon atoms.
  • R 4 is independently selected from the group consisting of alkyl, hydroxyalkyl, alkoxyalkyl and hydroxyalkoxyalkyl groups containing up to six carbon atoms.
  • R 4 comprise groups having up to six carbon atoms to facilitate rapid hydrolysis of the organooxysilane, which reaction is driven by the evaporation of the alcohol analog product of the hydrolysis.
  • R 4 groups having greater than six carbon atoms tend to impair the hydrolysis of the organooxysilane due to the relatively low volatility of each alcohol analog.
  • Particularly preferred organooxysilanes are trialkoxysilanes such as Union Carbide's A-163 (methyl trimethoxy silane), A-162 and A-137, and Dow Coming's Z6070 and Z6124.
  • a preferred coating composition comprises in the range of from one to ten percent by weight organooxysilane.
  • a flooring composition comprises up to about two percent by weight organooxysilane. If the coating and flooring composition comprises an amount of organooxysilane outside each range, the coating and flooring composition produced will display inferior impact resistance and chemical resistance.
  • a coating composition comprises approximately five percent by weight organooxysilane.
  • a flooring composition comprises approximately 0.7 percent by weight organooxysilane.
  • a commercially available resin part (including all ingredients) can be used in accordance with the present disclosure.
  • Can A is PSX 700 (from PPG) can be used as a resin part.
  • a resin part can then be mixed with a cure part.
  • a cure part may include at least one amino-silane and optionally a catalyst.
  • a first container prior to combining, includes a resin part, while a second container includes a cure part.
  • a catalyst can be combined and packaged with a cure part prior to mixing with a resin part.
  • a silane compound-based epoxy involves the reaction of an epoxide resin with amine to form a cured epoxy polymer, and hydrolyric polycondensation of polysiloxane and organooxysilane to produce alcohol and a polysiloxane polymer.
  • an aminosilane is utilized a cure part, a amine moiety of the aminosilane undergoes the epoxy-amine addition reaction and a silane moiety of the aminosilane undergoes hydrolytic polycondensation.
  • the resulting coating can exist as linear epoxy-modified polysiloxane which may have substantial advantages over conventional epoxy systems.
  • an amino-silane can be used in a cure part in accordance with the present disclosure.
  • Exemplary amino-silanes were listed and tested in Examples below.
  • suitable amino-silanes used in accordance with the present invention have the general formula: where R 11 and R 10 are independently selected from the group consisting of hydrogen, alkyl, hydroxyalkyl, alkoxyalkyl and hydroxyalkoxyalkyl groups containing up to six carbon atoms.
  • R 10 is hydrogen.
  • R 10 is hydrogen.
  • a cure part can be or comprise one or more aminosilanes.
  • DYNASYLAN 1189 CAS # 31024-56-3
  • DYNASYLAN DAMO CAS # 1760-24-3
  • any two aminosilanes can be used together in a cure part in a weight ratio of or more than about 0.1, about 0.3, about 0.5, about 0.8, about 1.0, about 1.2, about 1.3, about 1.4, about 1.5, about 1.6, about 1.7, about 1.8, about 1.9, about 2.0, about 3.0, about 5.0, about 10, about 20, about 30, about 40, about 50, about 100, or even about 200.
  • the weight ratio of any two aminosilanes can be in a range of about 0.1 to about 100, about 0.5 to about 20, or about 1 to about 10. In some embodiments, the weight ratio of any two aminosilanes can be in a range of any two values above.
  • DYNASYLAN 1189 CAS # 31024-56-3
  • DYNASYLAN DAMO CAS # 1760-24-3
  • an amino-silane having amine hydrogen milliequivalent weigh about or more than about 3 grams, about 4 grams, about 5 grams, about 7 grams, about about 10 grams, about 12 grams, about 13 grams, about 14 grams, about 15 grams or about 20 grams. In some embodiments, an amino-silane having amine hydrogen milliequivalent weigh in a range of about 4 to about 15 grams. In some embodiments, an amino-silane having amine hydrogen milliequivalent weigh in a range of any two values above.
  • a resin part has an epoxy equivalent weight in a wide range depending on the epoxy ingredients in the resin part.
  • the resulting mixture e.g., a formulation or mixed composition
  • the resulting mixture has an amine to epoxy equivalent weight ratio depending on the weight ratio of two parts.
  • the amine to epoxy equivalent weight ratio of a claimed paint composition is as set out in the claims.
  • the amine to epoxy equivalent weight ratio of a formulation useful in accordance with the present disclosure can be equal to, more than or less than about 2.10, about 2.15, about 2.20, about 2.25, about 2.30, about 2.35, about 2.40, about 2.45, about 2.50, about 2.55, about 2.60, about 2.65, about 2.70, about 2.75, about 2.80, about 2.85, about 2.90, about 2.95 or even about 3.00.
  • the amine to epoxy equivalent weight ratio of a formulation useful in accordance with the present disclosure can be equal to, more than or less than about 3.10, about 3.15, about 3.20, about 3.25, about 3.30, about 3.35, about 3.40, about 3.45, about 3.50, about 3.55, about 3.60, about 3.65, about 3.70, about 3.75, about 3.80, about 3.85, about 3.90, about 3.95 or even about 4.00.
  • the amine to epoxy equivalent weight ratio of a formulation useful in accordance with the present disclosure can be equal to, more than or less than about 4.10, about 4.15, about 4.20, about 4.25, about 4.30, about 4.35, about 4.40, about 4.45, about 4.50, about 4.55, about 4.60, about 4.65, about 4.70, about 4.75, about 4.80, about 4.85, about 4.90, about 4.95 or even about 5.00.
  • the amine to epoxy equivalent weight ratio of a formulation is in a range of about 1.10 to about 1.50, about 1.20 to about 1.30, or about 1.20 to about 1.25.
  • the amine to epoxy equivalent weight ratio of a formulation is in a range of about 2.10 to about 2.85, about 2.20 to about 2.70, or about 2.30 to about 2.60. In some embodiments, the amine to epoxy equivalent weight ratio of a formulation is in a range of about 2.20 to about 3.00, about 2.40 to about 2.90, or 2.50 to about 2.75. In some embodiments, the amine to epoxy equivalent weight ratio of a formulation is in a range of about 2.10 to about 3.00 or about 2.45 to about 2.60. In some embodiments, the amine to epoxy equivalent weight ratio of a formulation is in a range between (and optionally inclusive of) a lower value and an upper value.
  • the lower value is about 1.0, about 1.1, about 1.2, about 1.25, about 1.3, about 1.35, about 1.4, about 1.45, about 1.5, about 1.55, about 1.6, about 1.65, about 1.7, about 1.75, about 1.8, about 1.85, about 1.9, about 1.95, about 2.0, about 2.05, about 2.1, about 2.15, about 2.2, about 2.25, about 2.3, about 2.35, about 2.4, about 2.45, or about 2.5; in some instances, the upper value is about 1.25, about 1.3, about 1.35, about 1.4, about 1.45, about 1.5, about 1.55, about 1.6, about 1.65, about 1.7, about 1.75, about 1.8, about 1.85, about 1.9, about 1.95, about 2.0, about 2.05, about 2.1, about 2.15, about 2.2, about 2.25, about 2.3, about 2.35, about 2.4, about 2.45, about 2.5, about 2.55, about 2.6, about 2.65, about 2.7, about 2.75, about 2.8, about 2.85, about
  • the mixing of a cure part with a resin part dictates the weight percentage of each ingredient or part in a formulation.
  • the weight percentage of a resin part can be in a wide range.
  • the weight percentage of a resin part in a formulation used in accordance with the present disclosure can be or more than about 0.1 wt%, about 1 wt%, about 10 wt%, about 20 wt%, about 30 wt%, about 35 wt%, about 40 wt%, about 45 wt%, about 50 wt%, about 55 wt%, about 60 wt%, about 65 wt%, about 70 wt%, about 75 wt%, about 80 wt%, about 85 wt%, about 90 wt%, about 95 wt%.
  • the weight percentage of a resin part in a formulation can in a range of about 10 wt% to about 90 wt%, or about 80 wt% to about 90 wt%. In some embodiments, the weight percentage of a resin part in a formulation can in a range of any two values above.
  • one or more catalysts can be added in a cure part.
  • Useful catalysts include metal driers well known in the paint industry e.g. zinc, manganese, cobalt, iron, lead and tin, each in the form of octoates, neodecanates and napthenates.
  • Suitable catalysts include organotin catalysts having a general formula, R 5 Sn(R 6 )(R 7 )(R 8 ), are selected from a group consisting of alkyl, aryl, and alkoxy groups having up to eleven carbon atoms, and R 7 and R 8 can be selected from the same groups as R 5 and R 6 , or from a group consisting of inorganic atoms such as halogens, sulphur or oxygen.
  • Dibutyl tin dilaurate, dibutyl tin diacetate, organotitanates, sodium acetate, and aliphatic secondary or tertiary polyamines including propylamine, ethylamino ethanol, triethanolamine, triethylamine, and methyl diethanoi amine may be used alone or in combination to accelerate hydrolytic polycondensation of polysiloxane and silane compound.
  • up to about 10 wt% (of total) catalyst may be added with a cure part to a resin part to speed drying and curing of formulations described herein.
  • the weight percentage of a catalyst in mixture of a cure part and a resin part can be about or less than about 10 wt%, about 9 wt%, about 8 wt%, about 7 wt%, about 6 wt%, about 5 wt%, about 4 wt%, about 3 wt%, about 2 wt%, about 1 wt%, about 0.5 wt%, about 0.2 wt%, or about 0.1 wt%.
  • the weight percentage of a catalyst in mixture of a cure part and a resin part can be in a range of 1-0.1 wt%. In some embodiments, the weight percentage of a catalyst in mixture of a cure part and a resin part can be in a range of about 10 to about 0.1 wt%, about 7 to about 0.5 wt%, or about 5 to about 1 wt%. In some embodiments, the weight percentage of a catalyst in mixture of a cure part and a resin part can be in a range of any two values above.
  • a hybrid system typically is an admixture of two types of resins.
  • the hybrid system can either be a hybrid polymer system in a homogeneous medium or a hybrid polymer system in a non-homogeneous medium (e.g., a hybrid dispersion).
  • Hybrid systems can contain two classes of different polymers or resins which interact cooperatively to provide desired properties, possibly in a solvent-based carrier.
  • the hybrid material in a solvent-based carrier can be part of a one component or a two-component coating material.
  • the coating 14 can be formed from a material in a liquid carrier.
  • the liquid carrier includes less than about 10%, and more preferably less than about 5%, and most preferably less than about 1% by volume/weight of any solvent-based carrier, e.g., an organic solvent.
  • any solvent-based carrier e.g., an organic solvent.
  • Exemplary solvents when optionally present, can include 2-butoxyethanol, ethylene glycol, ethyl benzene, xylenes, methyl amyl ketone, isopropyl alcohol, propylene glycol monomethyl ether, ethylene glycol monobutyl ether, butanol, paraffins, alkanes, polypropylene glycol, Stoddard solvent, toluene, ethoxylated alkylphenol, 1-methyl-2-pyrrolidinone, or 1-ethylpyrrolidin-2-one.
  • the solvent can be or includes hydrocarbons (such as saturated hydrocarbons and unsaturated hydrocarbons), alcohols (such as alkoxy alcohols, ketonic alcohols), ketones, esters (such as acetates), glycol ethers, and glycol ether esters.
  • hydrocarbons include toluene, xylene, naphtha (petroleum), petroleum distillates, ethyl benzene, trimethyl benzenes, and fractions of hydrocarbon mixtures obtained from petroleum refineries. Mixtures of any two or more of these solvents may also be utilized.
  • alcohols examples include ethanol, n-propanol, iso-propanol, n-butanol, iso-butanol, benzyl alcohol, 2-(n-propoxy)ethanol, 2-(n-butoxy)ethanol, 3-(n-propoxy)ethanol, and 2-phenoxyethanol. Mixtures of any two or more of these solvents may also be utilized.
  • ketones include acetone, methyl ethyl ketone, methyl n-propyl ketone, methyl n-butyl ketone, and methyl isoamyl ketone. Mixtures of any two or more of these solvents may also be utilized.
  • esters include ethyl propanoate, ethyl butanoate, ethyl glycolate, propyl glycolate, butyl glycolate, and isoamyl glycolate, methyl acetate, ethyl acetate, n-butyl acetate, isoamyl acetate, and t-butyl acetate. Mixtures of any two or more of these solvents may also be utilized.
  • Accelerators are agents that speed up the curing process.
  • Exemplary accelerators that can be used in the formulation include dibutyltin dialkanoate (e.g., dibutyltin dialaurate, dibutyltin dioctoate), and oxazolidine.
  • Acid promoters are also optional agents that speed up the curing process. Acid promoters include aryl, alkyl, and aralkyl sulfonic acids; aryl, alkyl, and aralkyl phosphoric and phosphonic acids; aryl, alkyl, and aralkyl acid pyrophosphates; carboxylic acids; sulfonimides; mineral acids and mixtures thereof.
  • sulfonic acids include benzenesulfonic acid, para-toluenesulfonic acid, dodecylbenzenesulfonic acid, and naphthalenesulfonic acid.
  • aryl, alkyl, and aralkyl phosphates and pyrophosphates include phenyl, para-tolyl, methyl ethyl, benzyl, diphenyl, di-para-tolyl, dimethyl, di-ethyl, dibenzyl, phenyl-para-tolyl, methyl-ethyl, phenyl-benzyl phosphates and pyrophosphates.
  • carboxylic acids include citric acid, benzoic acid, formic acid, acetic acid, propionic acid, butyric acid, dicarboxylic acids such as oxalic acid, and fluorinated acids such as trifluoroacetic acid.
  • sulfonimides include dibenzene sulfonimide, di-para-toluene sulfonimide, methyl-para-toluene sulfonimide, and dimethyl sulfonamide.
  • mineral acids include phosphoric acid, nitric acid, sulfuric acid and hydrochloric acid. In some embodiments, phosphoric acid, citric acid or a combination thereof can be utilized as an acid promoter.
  • Surface additives can modify the surface characteristics (such as surface tension properties, substrate wetting, gloss, feel, and slip) of the writable-erasable surface 16.
  • Examples of surface additives can include modified polydimethyl siloxanes and polytetrafluoroethylene.
  • the curable compositions can also contain other optional ingredients such as fillers, surfactants, light stabilizers, pigments, opacifying agents, defoaming agent, surface gloss-modifying agent, biocides, viscosity-modifying agent, dispersing agents, reactive diluents, extender pigments, inhibitors for corrosion or efflorescence, flame retardants, intumescent agents, thermal agents for energy efficiency, additives for protection from UV and/or IR, self-cleaning agents, perfumes, or odor sustaining agents.
  • other optional ingredients such as fillers, surfactants, light stabilizers, pigments, opacifying agents, defoaming agent, surface gloss-modifying agent, biocides, viscosity-modifying agent, dispersing agents, reactive diluents, extender pigments, inhibitors for corrosion or efflorescence, flame retardants, intumescent agents, thermal agents for energy efficiency, additives for protection from UV and/or IR, self-cleaning agents, perfumes, or odor sustaining agents.
  • TINUVIN® benzotriazole, triazine, or hindered amine based
  • CHIMASSORB® benzophenone based
  • wetting agents can modify the viscosity characteristics of the coating formulations.
  • wetting agents can include silicone free family of agents, Metolat® available from Munzing Chemie GmbH.
  • opacifying agents can include zinc oxide, titanium dioxide, silicon dioxide, Kaolin clay, e.g., high whiteness Kaolin clay, or mixtures thereof.
  • Defoaming agents can release the trapped air in the coatings and can enhance the surface smoothness.
  • Examples of defoaming agents can include polyethylene glycols, or silicone surfactants, e.g., polyether modified polydimethyl siloxane.
  • Defoaming agents such as the BYK family of agents are available from BYK-Chemie GmbH.
  • viscosity modifying agents examples include polyurethanes, or a commercial acrylic copolymer, TAFIGEL®, available from Munzing Chemie GmbH.
  • a formulation or mixed composition can contain up to 30 wt% of one or more modifying agents.
  • the weight percentage of a modifying agent in a formulation or mixed composition can be about or less than about 30 wt%, about 25 wt%, about 20 wt%, about 15 wt%, about 10 wt%, about wt%, about 8 wt%, about 7 wt%, about 6 wt%, about 5 wt%, about 4 wt%, about 3 wt%, about 2 wt%, about 1 wt%, about 0.5 wt%, about 0.2 wt%, or about 0.1 wt%.
  • the weight percentage of a modifying agent can be in a range of about 30 to about 20 wt%, about 20 to about 10 wt%, about 10 to about 1 wt%, or about 1 to about 0.1 wt%. In some embodiments, the weight percentage of a modifying agent can be in a range of about 30 to about 0.1 wt%, about 10 to about 0.5 wt%, or about 5 to about 1 wt%. In some embodiments, the weight percentage of a modifying agent can be in a range of any two values above.
  • one or more modifying agents including the examples described herein can be provided in a resin and/or cure part before mixing of the two parts.
  • titanium dioxide can be provided in a resin and/or cure part.
  • agents including but not limited to silicon dioxide or silica (e.g., Sylysia 350), aluminum oxide, modified urea (e.g., Byk 410), micronized, organic polymer (e.g., Ceraflour 1000) and combination thereof can be added to a resin part (e.g., Can A of commercially available PSX 700 from PPG).
  • a degree of hydrophobicity is desirable on a dry-erase coating surface in order to provide sufficient chemical resistance to penetration from the dry erase marker solvents and pigments.
  • the present disclosure provides an insight that many siloxane compounds useful to generate coatings with appropriate hydrophobicity show unacceptable VOC contents (i.e., VOC contents above 100g/L or 140g/L).
  • a resin part as provided in the Can A of commercially available PSX 700 was utilized to be mixed with a cure part in this Example.
  • Each of these amino-silanes was separately combined with a resin part in three different amine to epoxy ratios (i.e., 3.0 to 1.0, 2.0 to 1.0 and 1.25 to 1.0).
  • Table 2 illustrates the mixtures made with dynasylan 1411 as an example to achieve different amine to epoxy ratios.
  • a practical method employed for determining superior vs. inferior dry erase performance was to actually write and erase using common commercial dry erase markers on small scale samples of painted out formulations.
  • samples were painted out using a standard nap roller and are evaluated for dry erase performance using the following subjective conditions: 1) eraseability - Does a conventional dry erase marker completely remove after application to the coating surface?; 2) staining - Does a conventional dry erase marker leave a permanent stain on the dry erase coating surface after application and removal?; and 3) ghosting - Following application and removal of a conventional dry erase marker is there a visible "ghost" of the original mark left on the dry erase coating?
  • Various components can be mixed and cured in the presence of at least an additive (e.g., catalyst, surface modifier, etc.).
  • an additive e.g., catalyst, surface modifier, etc.
  • Example 1 the mixtures of components described in Example 1 were mixed with an additive.
  • exemplary additives include two catalysts (dibutyltin dilaurate (DBTDL; CAS # 77-58-7 ) and K-Kat tin free, a zinc complex catalyst (XK614)) and a surface modifier (PF 159).
  • This Example describes additional or alternative testing and characteristics of amino-silanes for use in dry erase coating.
  • a resin part as provided in the Can A of commercially available PSX 700 (from PPG) was utilized.
  • Exemplary amino-silanes alone or mixed were provided as a cure part, which was then mixed with a resin part at three different amine to epoxy ratios.

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Claims (9)

  1. Farbzusammensetzung, umfassend:
    einen Harzanteil, umfassend ein Epoxy, ein Polysiloxan und ein Organooxysilan;
    einen Härtungsanteil, umfassend ein oder mehrere Aminosilane;
    wobei der Harzanteil und der Härtungsanteil so gestaltet und ausgewählt sind, dass sie, wenn sie miteinander kombiniert werden, wobei die Farbzusammensetzung ein Amin-Epoxid-Äquivalentgewicht in einem Bereich von 1,3 bis 5 aufweist, aushärten, um eine Oberfläche zu bilden, die mindestens eine Trockenlösch-Eigenschaft zeigt;
    wobei die Trockenlösch-Eigenschaft aus der Gruppe ausgewählt ist, die aus Folgendem besteht: einer durchschnittlichen Oberflächenrauhigkeit (Ra) von weniger als 7.500 nm;
    einer maximalen Oberflächenrauhigkeit (Rm) von weniger als 10.000 nm;
    einem 60-Grad-Glanz von mehr als 70;
    einem Kontaktwinkel von weniger als 150 Grad;
    einer Porosität von weniger als 45 Prozent;
    einer Bruchdehnung zwischen 10 Prozent und 100 Prozent;
    einer Sward-Härte von mehr als 3;
    einem Taber-Abriebwert von weniger als 150 mg/Tausend Zyklen;
    einer Durchbiegefestigkeit zwischen 101,6 und 609,6 µm (4 mils und 24 mils) und einer Kombination daraus, wie in der Beschreibung gemessen.
  2. Farbzusammensetzung nach Anspruch 1, wobei der Härtungsanteil ferner ein Trübungsmittel oder ein Pigment umfasst.
  3. Farbzusammensetzung nach Anspruch 1, wobei der Härtungsanteil weiterhin einen Katalysator umfasst.
  4. Farbzusammensetzung nach einem der vorhergehenden Ansprüche, wobei das Aminosilan ausgewählt ist aus 2-Aminoethyl-3-aminopropylmethyldimethoxysilan, n-Butyl-3-aminopropyltrimethoxysilan, 3-Aminopropylmethyldiethoxysilan, 3-Aminopropyltriethoxysilan, 2-Aminoethyl-3-aminopropyltrimethoxysilan oder einer beliebigen Kombination davon.
  5. Farbzusammensetzung nach einem der vorhergehenden Ansprüche, wobei die Oberflächenbeschichtung dadurch gekennzeichnet ist, dass, beim Schreiben auf ihre Oberfläche mit einem Markierungsmaterial, umfassend ein Farbmittel und ein Lösungsmittel, wobei das Lösungsmittel Wasser und/oder Alkohole, Alkoxyalkohole, Ketone, Ketonalkohole, Ester, Acetate, Mineralspiritus oder Mischungen davon umfasst, das Markierungsmaterial von der Oberfläche des beschreibbar/löschbaren Materials gelöscht werden kann, so dass es für mehr als 100 Schreib- und Löschzyklen an derselben Position im Wesentlichen unsichtbar ist.
  6. Farbzusammensetzung nach einem der vorhergehenden Ansprüche, wobei die Oberflächenbeschichtung durch eine Einwirkzeit von mindestens 4 gekennzeichnet ist.
  7. Farbzusammensetzung nach einem der vorhergehenden Ansprüche, wobei die Farbzusammensetzung flüchtige organische Verbindungen (VOCs) von weniger als 140 g/L aufweist, bestimmt nach der EPA-Methode 24.
  8. Farbzusammensetzung nach einem der vorhergehenden Ansprüche, wobei die Farbzusammensetzung VOCs von weniger als 100 g/L aufweist, bestimmt nach der EPA-Methode 24.
  9. Farbzusammensetzung nach einem der vorhergehenden Ansprüche, wobei sich der Harzanteil in einem ersten Behälter und der Härtungsanteil in einem zweiten Behälter befindet.
EP13738034.1A 2012-01-20 2013-01-21 Trockene siloxanbasierte löschbare beschichtungen mit geringem gehalt an flüchtigen organischen komponenten Active EP2804917B1 (de)

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HK1198483A1 (en) 2015-05-08
AU2013209470B2 (en) 2016-05-12
SG11201404209TA (en) 2014-08-28
EP2804917A1 (de) 2014-11-26
US20150018455A1 (en) 2015-01-15
CA2862013A1 (en) 2013-07-25
WO2013110046A1 (en) 2013-07-25
JP2015511250A (ja) 2015-04-16
AU2013209470A1 (en) 2014-08-07
US9493029B2 (en) 2016-11-15
EP2804917A4 (de) 2015-09-30
MX2014008760A (es) 2015-02-10

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